Processes for sulfur curing ethylene/vinyl chloride copolymers



Patented Dec. 5, 1995? 3,356,658 PROCESSE FQR SULFUR CURING ETHYLENE/ VINYL CHLORIDE CQPOLYMERS Harry M. Andersen, Ballwin, Harry P. Holladay, Creve Coeur, and John H. .Folrnson, Kirliwood, Mm, assignors to Monsanto Company, a corporation of Delaware No Drawing. Filed (lot. 21, 1963, Ser. No. 317,764

17 Gaims. (Cl. 260-795) This invention relates to processes for sulfur curing ethylene/vinyl chloride copolymers to form elastomeric materials having improved strength, elongation, dimensional stability, solvent resistance, etc.

Ethylene/ vinyl chloride copolymers may be prepared by conventional mass, emulsion, solution, or suspension polymerization techniques and initiation may be by either thermal dissociation of a suitable peroxy compound, by a redox system, or with ionic and Ziegler type catalysts. Reference is made to U.S. 2,422,392, U.S. 2,497,291, U.S. 3,035,032, and U.S. 3,051,689 for specific examples of processes for preparing the copolymer.

The art on curing these copolymers comprises U.S. 2,497,291 which states that curing agents may be added to ethylene/ vinyl chloride copolymers and U.S. 2,628,214 which further suggests that copolymers of ethylene and vinyl chloride can be crosslinked with free-radical-generating curatives, e.g., peroxides.

It is an object of the present invention to provide a new and more useful process for crosslinking ethylene/vinyl chloride copolymers.

Another object of this invention is to provide a process for curing ethylene/ vinyl chloride copolymers which process produces a product having superior properties to the product formed with a peroxide-type cure system.

Another object is to provide, as a composition of matter, ethylene/ vinyl chloride copolymers which have been vulcanized with sulfur according to the present processes.

Another object is to provide a process for vulcanizing ethylene/ vinyl chloride copolymers which process is suitable for commercial operations.

Another object is to provide a process for curing ethylene/vinyl chloride copolymers which is applicable whether or not fillers and/or plasticizers are employed to modify the resin.

Another object is to provide a process for crosslinking ethylene/ vinyl chloride copolymers to give elastorners having high tensile strengths and elongations.

Another object is to provide a process for preparing ethylene/vinyl chloride vulcanizates wherein the ethylene/ vinyl chloride copolymer does not suffer degradation and decomposition during the crosslinking operation.

Another object is to provide a process for curing copolymers of ethylene and vinyl chloride where the cured product has useful physical properties over a wide temperature range.

The objects set forth above and others, which will be evident to those skilled in the art from the detailed description of the invention which follows, have been accomplished in a process which employs a sulfur cure system to produce crosslinked ethylene/vinyl chloride copolymers.

It was most surprising that such a process could be developed, considering that sulfur cure systems will not function to crosslink seemingly related polymers, i.e., polyethylene, polyvinyl chloride, ethylene/vinyl acetate copolymer, etc.

The ethylene/vinyl chloride copolymers included within the scope of this invention have properties ranging from modified polyethylene to modified polyvinyl chloride. Copolymer compositions can contain about 5 mole percent vinyl chloride up to about 95 mole percent vinyl chloride and include semicrystalline polymers, i.e., those with about 5 to 20 mole percent vinyl chloride; rubbery polymers, i.e., those with about 20 to 40 mole percent vinyl chloride; soft thermoplastics, i.e., those with about 40 to 60 mole percent vinyl chloride; and semi-rigid to rigid thermoplastics, i.e., those With about 60 to 95 mole percent vinyl chloride.

Preferred ethylene/vinyl chloride compositions for use in preparing vulcanizates are the rubbery and soft thermoplastic polymers, i.e., those which contain from about 20 to 65 mole percent vinyl chloride. However elastomers having more or less combined Vinyl chloride may be preferred for certain applications.

Vulcanizable ethylene/vinyl chloride compositions usually contain fillers (i.e., diluents, reinforcing agents, pigments, etc.) which are used to extend or modify the basic copolymer.

, Carbon black is often added to the ethylene/vinyl chloride copolymer during compounding as a filler. There are many types of carbon blacks used today as fillers, among which are super abrasion furnace blacks, intermediate super abrasion furnace blacks, semi-reinforcing furnace blacks, very fine furnace blacks, high elongation furnace blacks, conductive furnace blacks, fully reinforcing furnace blacks, high abrasion furnace blacks, general furnace blacks, and high modulus furnace carbon blacks; all-purpose channel blacks, conductive channel blacks, easy processing channel blacks, medium processing channel blacks, and hard processing channel blacks; fine thermal blacks and medium thermal blacks; lamp blacks; acetylene carbon blacks, etc.

Other common fillers which can be employed include Wood flour, shell flour, cotton flock, signal fibers, chopped paper, macerated fabrics, keratin products, lignin fillers, soybean meal, synthetic fibers, asbestos, mica, quartz, limestone, silica, clays, diatomaceous earth, fibrous glass, calcium carbonate, calcium silicate, alumina, zinc oxide, barium sulfate, titanium dioxide, talc, cork, carborundum, iron oxide, zinc sulfide, etc.

As a general rule best strength is achieved where the filler is employed in about parts per 100 parts of copolymer. However, this value is only a guideline and from about 25 to parts filler may be preferred for certain applications. As little as about 1 to 10 parts can sometimes be used to advantage. On the other hand for certain applictaions best economic advantage is attained by adding from about 250 to 550 parts filler.

Additionally common plasticizers (i.e., softeners) can advantageously be added to modify the ethylene/vinyl chloride copolymers. Examples include phosphoric acid esters, esters of phthalate acid, esters of adipic acid, esters of azelaic acid, esters of oleic acid, esters of sebacic acid, palm oil, rape oil, olive oil, linseed oil, castor bean oil, soya bean oil, tung oil, mineral rubbers, high boiling petroleum residues, asphalts, pine tar, paraifin wax, mineral oils (aromatic, paraffinic or naphthenic), coal tar oils, fatty acids, naphthalenes, rosin, wool grease, carnauba wax, ceresin, glycerol esters, coumarone resins, styrene resins, phenol-formaldehyde resins, esters of fumaric acids, polyphenyls, chlorinated polyphenyls, chlorinated polyethylene, aromatic fractions from petroleum, butyl rubber, etc.

These plasticizers are generally added to the vulcanizable copolymers only to a limited extent, i.e., in amounts sufiicient to produce the desired properties. Commonly the amount of plasticizer used comes to about to 30 parts based on 100 parts of copolymer. However, as little as 1 to 5 parts may be effective. Also sometimes special conditions require as much as about 60 parts.

The sulfur is generally used in the elemental form as the ground sulfuf of commerce. Sulfur compounds ca-.

pable of liberating sulfur at vulcanizing temperatures are also used to effect vulcanization. The principal members of this group are bis(dimethylthiocarbamoyl)disulfide and its homologs, the corresponding tetrasulfide, dipentamethylene tetrasulfide, 4,4'-dithiodimorpholine, alkyl phenol sulfides, sulfur chloride, hydrogen sulfide, sulfur thiocyanate, etc. Sulfur compounds should be soluble in the copolymer or available in a finely divided form so that they can be readily and uniformly dispersed in the copolymer.

A typical formulation would include about 0.5 to 5 or more parts of sulfur for each 100 parts of crosslinkable copolymer. Generally about 1 to 3 parts of sulfur provides satisfactory crosslinking. Where a sulfur containing compound is used as the source of sulfur its sulfur content should fall within the above designated range.

Accelerators are added to the crosslinkable ethylene/ vinyl chloride copolymer to increase the rate of vulcanization. In general good accelerators also give flatter cures, improve tensile strength, set, hysteresis, and aging, and make possible a wider range in the combination of properties obtainable. Accelerators can be divided into 4 principal chemical groups: mercaptothiazoles and derivatives; dithiocarbamates and bis(thiocarbamoyl)sulfides, i.e., the thiuram sulfides; guanidines; and aldehyde-amine reaction products. A fifth miscellaneous group comprises various classes generally of secondary importance, e.g., xanthates, thioureas, and mercaptothiazolincs. Specific examples include: 2-mercaptobenzothiazole, 2,2-dithiobenzothiazole, N-cyclohexyl-Z-benzothiazolesulfenamide, zinc diethyldithiocarbamate,tetramethylthiuram disulfide, tetramethylthiuram, monosulfide, 1,3-diphenylguanidine, butyraldehyde-aniline condensation product, tellurium diethyldithiocarbamate, selenium diethyl dithiocarbamate, zinc dimethyl dithiocarbamate, etc. The dithiocarbamates and the bis(thiocarb'amoyl)sulfides function as ultra-accelerators and are preferred for present purposes.

The accelerator or the combination of accelerators is generally used in an amount about equal to 2 times the amount of sulfur in the cure formulation, however more or less may be used. Thus commonly the cure formulation will contain from about 0.5 to 5 parts of accelerator(s) per 100 parts of copolymer. Preferably'however, there will be from about 1 to 3 parts of accelerator(s) in the cure recipe.

Where desired activators, e.g., stearic acid, aniline, animal fatty acid, antimony sulfide, caprylic acid, coconut fatty acid, diethan'olamine, hydroxystearic acid, basic lead carbonate, lead salicylate, oleic acid, p-quinone dioxim'e, ricinoleic acid, tetrachlorobenzoquinone, zinc stearate, lead carbonate, lead oxide, magnesium oxide, etc., can be included in the cure recipe. These substances generally are not accelerators when used alone,

but inconjunction with a primary accelerator they in-- crease the rate of vulcanization over that which is obtained with only the primary acceleraton. The general argument for the use of an activator is that a fast cure rate may be obtained more economically by using a combination of accelerator and activator than by using a higher concentration of the accelerator. One to 3 parts of activator based on 100 parts of copolymer is generally sufficient for this purpose though more is desirable in some cases.

In most cases, it is the practice to add stabilizers to zinc palmitate,.

the vulcanizable ethylene/vinyl chloride copolymer during the mixing step of processing in order to prevent, retard, or modify to an unobjectionable form, degradation that might take place during processing and/or give satisfactory service life to the polymer by preventing or retarding degradation during use caused by the effects of oxidation, heat or light.

Many classes of compounds would be useful stabilizers of the present compositions. These include substituted phenols and bisphenols, amines, mercaptides and sulfides, phosphites, epoxies, phosphates, polyols, and inorganic and organometallic compounds. Since reactions which take place during polymer degradation are caused by a variety of factors, often a multicomponent stabilizer system will be useful.

Examples include the following: diphenylamine; reaction products of acetone with aniline or substituted anilines; reaction products of diphenylamine with acetone; derivatives of p-phenylenediamine; phenols alkylated with isobutylene or styrene; alkylated di-phenolics; reaction products of sulfur chloride and alkylatedphenols, alkylated .aryl phosphites; epoxidized natural oils; epoxidized esters of unsaturated acids; epoxy resins, pentacrythritol, glycerine, organometallic compounds based upon sodium, calcium, barium, strontium, cadmium, zinc, antimony, tin, lead, magnesium, aluminum and titanium; inorganic lead salts such as carbonates and silicates; etc.

The sum total of stabilizer(s) incorporated into the copolymer generally does not exceed about 10 parts per hundred parts of copolymer and usuallyis about 1 to 5 parts.

The vulcanizable ethylene/vinyl chloride copolymer is cured by applying heat thereto until the desired degree of crosslinking is achieved. Cure temperature depends on the accelerator employed and will generally be on the order of about to 450 Fahrenheit. The preferred temperature range is from about 250 to 350 Fahrenheit.

The cure time depends on the cure temperature, i.e., where high temperatures are employed the optimum cure time will be shorter than when the copolymer is vulcanized at lower temperatures. vulcanization time also depends on the size of the sample being cured, the presence or absence of an activator, the particular accelerator employed, etc. However, vulcanization time will usually be on the order of about /3 to 150 minutes. Optimum cure time at about 320 Fahrenheit is usually about 15 to 45 minutes.

The crosslinked copolymers prepared by this invention have utility for many purposes, e.g., coatingsfabrics and paper; as water resistant adhesives; for the preparation of molded articles; safety glass interlayers; protective coatings for vats, tanks, food cans, etc.; wire insulation, elastomeric materials; etc.

Various changes may be made in the details of this invention without departing therefrom or sacrificing any of the advantages thereof. For example it is possible to cure ethylene/vinyl chloride polymers containing a third polymer component under conditions substantially the same as hereinbefore described. The third component should not be present in an amount exceeding about 15 weight percent based on the combined monomers.

In the following examples E/VCl is used as an abbreviation for ethylene/vinyl chloride copolymer. The superscript t is used to denote a trademark or brand name.

EXAMPLE l.-BUTYL-SULFUR CURES OF E/VCl A typical butyl rubber cure system was used to cure E/VCl latex (Table 1). Films of the cure formulation are cast on glass and allowed to dry overnight before curing. The degree of cure obtained is indicated by the insolu bility of the cured film in 50:50 methyl isobutyl ketonetoluene solvent.

3,356, 658 e TABLE l.E/VCl LATEX RUBBER OURES [E/V C1 Latex-57.0 mole percent V01, 50.6% polymer solids] 100 0. 5 1. 0 2. 0 2. 0 Steari 1. 0 Cure:

Time (min) 30 30 60 30 30 60 Temp. F. 320 302 302 320 302 302 Solubility: 50: 50 methyl isobutyl ketoneene Sol. Sol. Sol. Insol. Partly Insol. (Swelled) Sol. (Swelled) l Thiotax=2-mercaptobenzothiazole; Thiurad=tetramethylthiuram dlsulfide.

Additional results of butyl-type sulfur cures (i.e., sulfur cures with accelerators) are presented in Table H. A with solid E/VCI at 50 parts loading was made to deterpentaerythritol-ZnO system is employed as stabilizer. mine ones yielding best physical properties (Table III).

TABLE II.BUTYL-SULFUR CURES OF E/VCl Mole percent VCl in E/VCl 41 41 53. 4 53. 4 34. 8 34. 8 57, 7 Cure Formula: a

Polymer 100 100 100 100 100 100 100 Philblack O 50 50 50 50 Stearic Acid 1 1 1 1 1 1 ZnO 5 5 5 5 5 Sulfur 1 5 6 1 5 1 1. 2 2 1 2 1 1 1 2 2. 60 3. 7. Optimum Cure (1pm.) 20.80 46.1 Press Cure Results: 0

Cure Temp. F.) 310 310 310 310 310 310 310 290 290 Cure Time (min.) 19 20 15 7 5 10 20 Percent Elong 520 175 48 183 173 173 263 297 240 Percent Retained Elong. 12 8 0 24 18 14 17 27 13 Tensile, lbs/in. 2 2,070 3,300 1, 462 1,670 1,721 1, 703 2,663 2,325 2, 750 Philblack O =high abrasion oil furnace black; Tellurac=tellurium di- Cure time=t +6Atm ASTM D1646-59l. ethyldithiocarbamate; Mcrtax=2-rnercaptobenzothiaz01e; Elastopar= ASTM D412-51T, Dre C. N -methyl-N 4-dinitrosoaniline (1 part) plus clay filler (2 parts).

N0 degradation or HCl evolution is noted and fast cure rates are the rule. The stock has 58 mole percent VCl and is plasticized With dioct l hthalate to r v'de 00d 1 W t m ra r EXAMPLE 2.FILLED-CURED E/VCl STOCKS y P P 0 1 g e P6 e PmPer ties to minimize decomposition. Otherwise the cure formu- A study of varying types of black and non-black fillers lation shown in Table 1 was followed,

TABLE III.FILLERS FOR E/VCI 15 min. cure at 310 F. 25 min. cure at 310 F. Filler (50 parts, hpr.)

Tensile, Elong., Perm. Tensile, Elong., Penn.

p.s.i. percent Set, percent lbs/in. percent Set, percent None, Control 1, 355 527 2. 75 808 493 2. 36 Black Fillers: 2

Pliilblack O 1 2, 252 323 5. 47 2, 287 310 6. 45 Philblack E t 2, 660 307 6.07 2, 850 280 6.07 Philblack I L 2, 328 327 6.12 2, 560 307 5. 22 Regal 300 k 2, 318 360 5. 18 2, 535 357 5. 08 Sterling V 1, 823 363 4. 41 2, 060 347 4. 13 Black Pearls 81 2, 265 220 4. 32 1, 307 6.17 Spheron 6 2, 765 360 5.00 1,873 177 3. 58 Spheron 9 2, 803 290 5. 17 2, 540 250 4.80 Thermax 1, 610 525 4.00 1, 668 437 3. 51 N on-Black Fillers: 3

McName Clay t 1, 686 538 10. 1, 980 580 8. 62 Calcene TM 2, 335 660 6. 37 2, 338 657 5. 37 Hi $11 233 1, 977 543 10.70 2,155 493 11.32 Ti Pure 610 t 2, 090 637 4. 71 2, 048 587 3. 71

1 58 mole percent VCl; softened with 15 parts DOP (dioctyl phthalate).

2 Philback E=super abrasion oil furnace black; Philblack I=intermediate super abrasion furnace carbon black; Regal=fully reinforcing oil furnace black; Sterling V=general purpose furnace black; Black Pearls 8l=regular color all-pmpose processing channel black; Spheron 9=easy processing channel black; Thennax=a medium thermal carbon black.

3 McName Clay=a soft kaolin clay; Calcene TM=precipital calcium carbonate coated with a rubber soluble agent; Hi Sil 233=hydrated silica pigment of extremely fine particle size; Ti Pure 610=rutile T102.

The furnace blacks give the highest degree of reinforcement and display relatively flat curves. The best reinforcement is by Philblack E and best elongations are obtained with Regal 300 Spheron 9 1; appears to be the best of the channel blacks.

Calcene TM is the best non-black reinforcer tested. However all non-black fillers give respectable properties with good elongations.

improve reinforcement, indicates that the heat treatment necessary to render Elastopar effective is unacceptable for E/VCl stocks.

Philblack E Regal 300 R and Calcene TM were chosen for further study of optimum loading of the E/VCl formulation. These results are given in Table IV.

TABLE IV.OPTIMUMFILLER LEVELS FOR ENC! min. cure at 310 F. min. cure at 310 F.

Filler Parts, Elong., Modulus, p.s.i. Shore Elong, Modulus, p.s.l. Shore hpr. Tensile, P.s.l., Per- Perm. A Tensile, P.s.i., Per- Perm. A

p.s.i. Yield cent Set Hard. p.s.i. Yield cent Set Hard.

1 Hardness determined with a Shore A Durometer; ASTM D676-49T.

Using Ph-ilblack O t as filler a study was made of pre-.

heat times in the mold prior to raising to full pressure.

Optimum loadings for Philblack E t and Calcene TM Specimen appearance and physical properties obtained are close to 50 parts based on achievement of highest using 90, 60, and 15 sec. of warm-up time in the press tensiles. The best performance for Regal 300 appears to at low pressure were noted. There is some evidence that be obtained with closer to 40 parts. cure has begun and flow is restricted at the sec. level.

Several formulation and curing condition variables were Best results are obtained at 60 and 30 sec. while 15 sec. investigated (Table V). is insufficient to heat to temperature for best flow.

TABLE V.MISCELLANEOUS E/VCl 5 FORMULATION STUDY 15 min. cure at 310 F. 25 min. cure at 310 F.

, Modulus Elong, Tensile Perm. Set, Elong., lbs/in. percent percent Variation otStandard Cure Formula 1 Tensile Perm. Set, lbs/in. percent percent ZnO, 30 parts hpr Ti-Pure, 20 parts hpr... 607 2,120

Philblaek E, 25 parts hpr. Cal'eene TM," 25 parts hpr Philblack E, +1.5 parts hpr. suliu 7.5 min. eure 15 min. cure 25 min. cure Philblack E, 50 phr Elastopar R, 1.5 phr Philblack 0, 50 parts-See. pre

prior to full pressure cure 1 Standard Formula Ingred:

Parts E/VCl-Sottener Zn 5 Stearic Acid 2 Suliur 1. 25 Thiurad t 1. 5 Mertax 1 The effects of various potential stabilizers were determined using both 51-57 mole percent (Table VI) and 35 mole percent VCl copolymer, (Table VII). Performance is evaluated by an oven cure (30 min. at 310 F.)

The best stabilizers for prevention or" char and metal attack are, in a thiourea, pentaer Epoxol 9-5 dimeth fective additive appe ythritol pproximate order of their effectiveness: glycerine, Resimene U920 ylol urea, urea, etc. One part of cfars suilicient.

Stabilizer combinations were studied for prevention of with ca. sam les bein com ressed between rolled g p g p polymer decomposition and corrosive attack of molds. steel plates.

TABLE VI.-E/V0l CURE STABILIZERS FOR 51-57 MOLE PERCENT VCl COPOLYMER Metal Plate Char Test 2 Run Stabilizer (1 phr. for each additive) 1 El0ng., Permanent Tensile, Percent Set, Percent lbs/in.

Char Ring Metal Attack Color A. 57% V01 copolymer with pts. DOP (dioctyl phthalate) cured min. at 310 F.

I 1 N one-control Charred on cure 100% H. Brn Pentaerythritol 627 2. 77 1,849 V.Sl. V.Sl. Lt. Glyceryl monolaurate. 540 l. 69 1,284 M. M. Glycerine 650 2. 77 1, 924 V.Sl. S1. Lt. Advastab CHI-300 520 2. 31 980 100% H. Brn. Quadrol t N o cure N 0 char glvanol 70505 1.- 573 2. 74 1, 408 g H. M.

entaeiyt rito {salmowhite Crystals 647 2.83 1,172 B" v. s1. Lt.

ycerine 9 santowhite Crystals t J 646 2. 81 2, 023 Li. S]. Lt. Santowhite Crystals 467 1. 78 860 100% H. Bin.

B. 51% VCl Copolymer with 15 pts. DNODA [di(n-octyl, n-decyDadipate]; cured 25 min. at 310 F.; Additive (2 pts.)

Resimcne U-920 t 670 2. 59 1, 696 V. 81. None Lt. Epoxol 9-5 700 2. 62 2, 048 $40 51. t. Urea 627 3. 56 920 None Sl. Lt. Thiourea 650 3. 33 1, 321 do None Lt. Sucrose octa-acetate 623 2. 35 1, 800 H. Lt. Dimethylol urea 657 3. 04 l, 431 %2 V. S]. Lt. Glycerine 667 3. 15 l, 499 Trace V. Sl. Lt. N one-control 627 2. 50 1,820 A6 H. Brn 1 Advastab OH-300=an organic phosphite; Quadrol=reaction product formaldehyde resin; Epoxol 95=epoxidized soybeam oil. of ethylene diamine with 4 molecules of propylene oxide; Elvanol 70-05- 2 Approximately $4 g. samples, cured min. at 310 F., in direct conpartially hydrolyzed polyvinyl acetate; Santowhite Crystals=4,4- tact with rolled-steel plates; Sl.=slight; V. Sl.=very slight; M.=moderthiobis-(o-tert-butyl-meta-cresol); Resimene U920=a butylated ureaate; Lt.=11ght; H =heavy; Brn.=brown.

TABLE VIL-E/VCl CURE STABILIZERS FOR MOLE PERCENT V01 COPOLYMER Metal Plate Char Test 1 Run Stabilizer and Additives Cure Time Elong., Perm., Set, Tensile, (min.) Percent Percent lbs./in.

Char Ring Metal Attack Color A. (35% E/VOl) no plasticizer Stabilizer (2 phr.)

Dibasic lead phosphate 25 750 4. 63 Dibasic lead phosphate. 743 4. 26 Epoxo19-5 t 25 747 3. 53 d0 50 790 3. 42 Resim 25 667 2. 91 d0 50 680 2. 72 N one-control 25 657 2.

B. (35% E/VCl) compounded with 50 phr. Philblaclr E Additives Clash-Berg Properties 3 T1, C. T5000, C. SR, C. None 25 50 6. 0 1, 947 23 220 243 15 phr. DNODA 25 1. 25 828 41. 5 78 119. 5 15 pin. DNODA, 1 phi. U-920. 25 300 3. 00 1, 483 -40. 5 7 47. 5 1 Approximately g. samples, cured 30 min. at 310 F., in direct con- The Twin value is the tem hich the material becomes very tact with rolledsteel plates; V.Sl.=very slight; Lt.=1ight; H=heavy; Brn.=brown.

2 Clash-Berg modulus data gives information of the tors1onal stifiness of the polymer as related to temperature. The '1: value is the temperature at which the polymer just begins to have some slight degree offlexibihty.

3,356,658 1 1 1 2 Results (Table VIII) show thiourea and glycerine to be the presence of a sulfur cure system containing elemental most effective. Epoxol 9-5 1 also shows promising utility. sulfur.

TABLE VIII.CURE STABILIZERS 1 Metal Plate Oven Test 8 Run Stabilizer Elong., Perm. Set, Tensile,

Additives Percent Percent p.s.i.

Char Ring Metal Att. Color E 677 3. 25 1, 5 None None Pink G (V2) 003 2. 03 1,900 None V. Sl. Lt. G (V 663 2.72 1,709 1/32 V. Sl. Lt. E (%l 670 2. 69 1,811 1/8" 1/16" Lt. E (V 837 4.38 1,572 1/32 V. Sl. Lt. 'I 670 2. 64 1,798 1/32 V. S1. Lt. E 695 2.59 2,083 None V. Sl. Lt. E (V2) 603 2. 72 1, 652 None V. Sl. Lt.

E (1) 700 3.43 1,552 1/8 1/8 Pink T (1)- 680 4.02 1,510 Sl. V. Sl. Lt. G (1) 710 3. 52 1,271 Sl. V. Sl. Lt.

1 E IV 01 stock is 51 i nole percent VCl compounded with pts. DNO DA [di(n-octyl, n-decyl) adipate] and standard cure formula.

Cured min. at 310 4 2 Stabilizers as follows: E, Epoxol 9-5 G, glycerine; R, Resimene (l-920 S, Santowhite Crystals T, thiourea. Figures in parenthesis are parts per hundred parts of polymer.

3 Approximately g. samples, cured min. at 310 F., in direct contact with rolled-steel plates; Sl.:slight; V. Sl.:very slight;

Lt.=light.

Effects of stabilizers on cure rates were measured 25 (Table IX). Glycerine, Resimene U-920 and thiourea 2. The process of claim 1 Where the copolymer conretard cure rate to increasing degree in the order given. tains a filler.

TABLE IX.-CURE STABILIZERS 1 Mooney Cure 3 Physical Properties Metal Plate Oven Test 4 Run Stabilizer Additives 2 Temp., t5 tZm Time Cure Cure Elong., Perm. Tensile Char Metal I (min) (min) (min) Temp. Time, percent Set, (p.s.i.) Ring Att. Color F.) min. percent 1 Contr 310 20 620 1 61 1,650 Total H. BT11. 2 S (1/2) 1 310 25 47 2 11 1,594 3 S (1/2) T (1/2) E 310 033 2.37 1,117 S1 Lt. 4... E (1) S (1/2)--- 6 8 3 1 21. 310 20 603 2.42 1,473 H. Lt. 5 E (1) S (1/2) G (1/.. 310 7 6 4 5 34.6 310 35 677 1.77 1,514 None None Lt. 6 E (1) S (1/2) R (1/2)... 310 8 0 4 2 33.2 310 35 610 1.80 1,592

l EIVCl stock is 51 mole percent VCl compounded with 15 pts. are parts per hundred parts of polymer. DNODA [di(n-octyl, n-decyDadipate] and standard cure formula. 4 Approximately 1/4 g. samples, cured 30 min. at 310 F., in direct Cured 25 min. at 310 F. contact with rolled-steel plates; Sl.=slight; Lt.=light; H=heavy; Brn.=

2 Stabilizers as follows: E, Epoxol 9-5 G, glyeerine; R, Resimene brown. U-920 S, Santowhite Crystals T, thiourea. Figures in parenthesis Additional data on stabilization of E/VCl cures is given 3. The process of claim 1 where the copolymer conin Table X. Pentaerythritol dissolved in glyccrine shows tains a plasticizer. improved compatibility and imparted good stability. 4. The process of claim 1 where the cure temperature Black-filled stabilized compoundedstock have good peris on the order of about 150 to 450 Fahrenheit. formance in transfer molding. 5. A process according to claim 1 wherein said ethyl- TABLE X.-CURE STABILIZATION OF E/VCl (51 MOLE PERCENT VCl) Physical Properties Metal Plate Test 2 Cure Time Run Stabilizers l (phr.) (min. at

310" F.) Elong, Perm. Set, Tensile,- Ghar Metal Color Percent Percent lbs/in. Ring fin.) Attack 1 Epoxsgl 9-5 (0.5), Resimene "(I-920 25 617 1.94 1,648 V.Sl. Lt.

2 Epoxol 9-5 t (0.5), glycerine (0.5) 25 587 2. 72 920 V.S1. Lt.

3 AIB 25 617 1. 95 1,402 None Lt.

4 Pentaerythritol (0.5) gly erine (0.5)..- 25 680 1.62 1,784 S1. Lt.

5 Trimethylolpropane diallyl ether 70 V.Sl. Lt.

6 l Trirnethylolpropane monoallyl cther 140 .V.Sl. Lt.

SAIB=sueroso acetate iso utyrate. contact with rolled-steel plates; Sl.=slight; V.Sl.=very slight; Lt.= Approximately 1/4 g. samples, cured 30 min. at 310 F., in direct light.

What is claimed is: ene/vinyl chloride copolymer has about 20 to mole 1. A process for preparing crosslinked ethylene/vinyl percent polymerized vinyl chloride and wherein said sulchloride copolymer-s which comprises curing an ethylene/ for cure system comprises elemental sulfur and an activinyl chloride copolymer having about 5 to mole pervator.

cent polymerized vinyl chloride in the presence of a sta- 6. The process of claim 5 where the copolymer conbilizer selected from the group consisting of butylated tains about 1 to 10 parts of stabilizer per parts of urea-formaldehyde resin, pentaerythritol, glycerine, phecopolymer.

n01, bisphenol, urea, thiourea and dimethylolurea and in 75 7. The process of claim 5 where the, copolymer con- 13 taius about 0.5 to parts of sulfur and about 0.5 to 5 parts or" accelerator per 100 parts of copolymer.

8. The process of claim 5' where the cure temperature is on the order of about 150 to 450 Fahrenheit.

9. A process for preparing crosslinked ethylene/vinyl chloride copolymers which comprises curing an ethylene/ vinyl chloride copolymer which has about 20 to 60 mole percent vinyl chloride and which contains about 1 to parts per 100 parts of copolymer of a stabilizer selected from the group consisting of butylated ureaformaldehyde resin, pentaerythritol, glycerine, phenol, bisphenol, urea, thiourea and dimethylolurea with a sulfur cure system comprising about 0.5 to 5 parts of sulfur and about 0.5 to 5 parts of accelerator per 100 parts of copolymer where the cure temperature is on the order of about 150 to 450 Fahrenheit.

10. The process of claim 9 Where the copolymer contains from about 50 to 550 parts of filler.

11. The process of claim 9 Where the copolymer contains from about 10 to 60 parts of plasticizer.

12. The process of claim 9 where the sulfur cure system is also comprised of about 1 to 3 parts of activator.

13. The process of claim 9 where about 1 to 4 parts of sulfur and about 1 to 3 parts of accelerator is used.

14. The process of claim 9 where the cure temperature is in the range from about 250 to 350 Fahrenheit.

urea, thiourea and dimethylolurea with a sulfur cure system comprising about 1 to 3 parts of sulfur, about 1 to 3 parts of accelerator, and about 1 to 3 parts of activator per 100 parts of copolymer where the cure temperature is in the range from about 250 to 350 Fahrenheit.

16. The process of claim where the copolymer contains about to 100 parts of filler.

17. The process of claim 15 where the copolymer has about 10 to parts of plasticizer.

References Cited UNITED STATES PATENTS 7/ 1946 Berry et al. 260-795 3/1947 Lindsey et a1. 260-79.5

JOSEPH L. SCHOFER, Primary Examiner. D. K. DENENBERG, Assistant Examiner.

UNITED STATES PATENT OFFICE CERTIFICATE OF CORRECTION Patent No, 3,356,658 December 5, 1967 Harry M. Andersen et a1.

It is certified that error appears in the above identified patent and that said Letters Patent are hereby corrected as shown below:

Column 4 line 45 "l/5" should read 1/2 Column 4 line 46, "320" should read 310 Columns 5 and 6, TABLE 1, third column, line 5 thereof, "2.0" should read 4.5 same table, second column, line 1 thereof, opposite "E/VCl" insert 100 Columns 5 and 6, footnote to TABLE III, line 3 thereof, after "Regal" insert 300 Columns 7 and 8,

TABLE V, second column, line 5 thereof, "+l 607" should read 1,607

Signed and sealed this 10th day of March 1970.

(SEAL) Attest:

EDWARD M.FLETCHER,JR, WILLIAM E, SCHUYLER, JR. Attesting Officer Commissioner of Patents 

1. A PROCESS FOR PREPARING CROSSLINKED ETHYLENE/VINYL CHLORIDE COPOLYMERS WHICH COMPRISES CURING AN ETHYLENE/ VINYL CHLORIDE COPOLYMER HAVING ABOUT 5 TO 95 MOLE PERCENT POLYMERIZED VINYL CHLORIDE IN THE PRESENCE OF A STABILIZER SELECTED FROM THE GROUP CONSISTING OF BUTYLATED UREA-FORMALDEHYDE RESIN, PENTAERYTHRITOL, GLYCERINE, PHENOL, BISPHENOL, UREA, THIOUREA AND DIMETHYLOLUREA AND IN THE PRESENCE OF A SULFUR CURE SYSTEM CONTAINING ELEMENTAL SULFUR. 